PICOSURE Pro - Indonesia BPOM Medical Device Registration
PICOSURE Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603220068. The device is manufactured by CYNOSURE, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDIVA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
CYNOSURE, LLCCountry of Origin
United States
Authorized Representative
PT. MEDIVAAR Address
K-LINK TOWER, LEVEL 11, SUITE G. JL. Jend. Gatot Subroto Kav. 59A
Registration Date
Jan 14, 2022
Expiry Date
Jun 30, 2024
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Radiation Electromedics
SCULPSURE Laser System
CYNOSURE INC.
MEDILITE C6 Laser System
CYNOSURE LLC..
PICOSURE
CYNOSURE LLC
REVLITE Laser System
CYNOSURE, LLC.
CYNERGY
CYNOSURE, INC.
NEWPONG SONOQUEEN Focused Ultrasound Stimulator
NEWPONG CO.,LTD